Difference between revisions of "DRD4-RGC"
(→Central Projections) |
|||
Line 24: | Line 24: | ||
DRD4-DSGCs send their axons to two retinorecipient areas of the brain: the dorsal lateral geniculate nucleus (dLGN) and the superior colliculus (SC). For both areas, axon terminations are restricted to specific laminae. In the dLGN, DRD4-DSGC axons were limited to a lamina running along the lateral dLGN, while in the SC, axons terminated in the upper half of the stratum griseum superficialis (uSGS). Inputs to both dLGN and SC arise from the controlateral eye. | DRD4-DSGCs send their axons to two retinorecipient areas of the brain: the dorsal lateral geniculate nucleus (dLGN) and the superior colliculus (SC). For both areas, axon terminations are restricted to specific laminae. In the dLGN, DRD4-DSGC axons were limited to a lamina running along the lateral dLGN, while in the SC, axons terminated in the upper half of the stratum griseum superficialis (uSGS). Inputs to both dLGN and SC arise from the controlateral eye. | ||
+ | |||
+ | ==Behavioral Output== | ||
+ | |||
+ | ==History== | ||
==References== | ==References== |
Revision as of 01:50, 18 September 2015
DRD4-DSGCs are On-Off direction selective ganglion cells that respond to global posterior motion (backward motion in relation to the world). These cells were discovered in transgenic mice that express GFP under the control of the dopamine receptor 4 promoter (DRD4-EGFP). Interestingly, the GFP positive RGCs in this mouse line all have properties of On-Off DSGCs, and exclusively prefer posterior motion. This selective labeling of On-Off DSGCs allowed for previously uncharacterized brain circuitry and axonal connection pattern of a specific subset of On-Off DSGC.
Contents
Anatomy
DRD4-DSGC cells exhibit canonical morphological characteristics of On-Off DSGCs. They are bistratified, costratifying with starburst amacrine cell (SAC) processes. Their dendritic fields are egg-shaped and dendritic arbors exhibit "looping" patterns. Although their dendritic arbors are mostly symmetric, their somas tend to shift slightly away from the center of their dendritic fields. The cells form a regular mosaic with a relatively high coverage factor (2.99 on average) (Rivlin-Etzion et al., 2011).
Physiology
All DRD4-DSGC cells are strongly excited by posterior motion, or motion toward the nasal pole of the retina. ON and OFF responses are exhibited in response to flashes of a white spot centered on the soma. Responses to drifting graftings reveal strong posterior direction tuning that is more narrowly tuned compared to another type of posterior motion preferring DSGCs (TRHR-DSGC).
Molecular Marker
These posterior motion-preferring On-Off DSGCs (pDSGCs) are characterized by their expression of Drd4 (dopamine receptor D4). Drd4-GFP BAC transgenic mice express Drd4 prominently in the prefrontal cortex, and also in the ganglion cell layer (GCL) of the retina (Gong et al., 2003, Huberman et al., 2009). Upon further inspection of the retina, dendrites of the GFP positive cells of the Drd4-GFP mouse were found to stratify in two distinct bands in the inner plexiform layer (IPL), suggesting bistratification (Huberman et al., 2009). The GFP positive dendrites appeared to be costratified with processes of startburst amacrine cells (SACs).
Central Projections
DRD4-DSGCs send their axons to two retinorecipient areas of the brain: the dorsal lateral geniculate nucleus (dLGN) and the superior colliculus (SC). For both areas, axon terminations are restricted to specific laminae. In the dLGN, DRD4-DSGC axons were limited to a lamina running along the lateral dLGN, while in the SC, axons terminated in the upper half of the stratum griseum superficialis (uSGS). Inputs to both dLGN and SC arise from the controlateral eye.
Behavioral Output
History
References
Gong S, Zheng C, Doughty ML, Losos K, Didkovsky N, Schambra UB, Nowak NJ, Joyner A, LIblanc G, Hatten ME, Heintz N (2003). A gene expression atlas of the central nervous system based on bacterial artificial chromosomes. Nature 425, 917-925.
Huberman AD, Wei W, Elstrott J, Stafford BK, Feller MB, Barres BA (2009). Genetic identification of an On-Off direction selective ganglion cell subtype reveals a layer-specific subcortical map of posterior motion. Neuron 62, 327-334.
Rivlin-Etzion M, Zhou K, Wei W, Elstrott J, Nguyen PL, Barres BA, Huberman AD, Feller MB (2011). Transgenic mice reveal unexpected diversity of ON-Off direction selective ganglion cell subtypes and brain structures involved in motion processing. J Neurosci. 31, 8760-8769.